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4 - 7 days
Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.
0.3 mL (Note: This volume does not allow for repeat testing.)
NMR lipoprofile serum-separator tube (N° 60360). Other tubes should not be used as they may produce erroneous results.
Allow the sample to stand for 60 to 120 minutes to release the ECP in the cells prior to centrifugation. Separate the serum after 60 to 120 minutes and transfer to a plastic transport tube.
Nonserum sample received; non-Greiner tube collected; grossly hemolyzed or lipemic samples
Eosinophils are effector cells that play a role in allergic and nonallergic inflammation.1,2 The most prominent feature of these cells is large cytoplasmic granules, each containing four basic proteins, the most plentiful of which is eosinophil cationic protein (ECP).3 ECP is a protein with ribonuclease activity that is released during eosinophil activation. While the full physiologic role of ECP has not been completely defined, this protein has been attributed with cytotoxic, neurotoxic, fibrosis-promoting, and immune-regulatory functions.1,3,4 Studies suggest that ECP may play a role in regulating mucosal and immune cells and may directly fight parasitic, bacterial, and viral infections.3
ECP is often elevated in diseases in which an eosinophil-mediated tissue inflammation plays a role.1,3,5 Measuring ECP levels has been used to evaluate eosinophil-mediated allergic inflammation, asthma, and rhinitis.1 Levels can be increased during both seasonal and perennial rhinitis1,6 and may reflect current allergen exposure.1,6 In atopic dermatitis, ECP has been shown to correlate with the symptoms and total clinical score.7
Eosinophilic inflammation is a relatively common feature of asthma.4,6,8-10 Although not diagnostic for asthma, elevated ECP levels are thought to reflect the degree of asthma-related bronchial eosinophilic inflammation.6,11 Increased ECP levels correspond to symptom onset and can precede bronchial hyper-reactivity.1,4 ECP has been used to assess asthma severity and support the management of anti-inflammatory therapy.5,11,12 It should be noted, however, that ECP is better correlated to symptom score than to lung function parameters, especially in children with mild and moderate asthma.6
ECP levels can be increased in a number of gastrointestinal disorders, including eosinophil intestinal diseases (esophagitis, gastroenteritis, and colitis), gastrointestinal food allergy, and intestinal parasitoses.1 ECP levels can also be increased in non−IgE-mediated conditions, including nonallergic asthma with aspirin intolerance, respiratory infections, sinonasal polyposis, and idiopathic hypereosinophilia (HES) syndrome.1,3 ECP has also been used as a disease activity marker in Churg-Strauss syndrome (CSS), a condition that is also known as allergic granulomatosis or allergic angiitis.13 CSS is a disorder marked by blood vessel inflammation that can restrict blood flow to vital organs and tissues, sometimes permanently damaging them.1,12 In a recent study, Niccoli and coworkers showed that ECP levels independently predicted the severity of coronary artery disease in patients with angina.14
BD plastic serum-separator tubes should not be used as they will produce erroneous results.
Results for this test are for investigational purposes only by the assay's manufacturer. The performance characteristics of this product have not been established. Results should not be used as a diagnostic procedure without confirmation of the diagnosis by another medically established diagnostic product or procedure.
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